Average salary: $150,359 /yearly
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- ...Job Title Responsibilities: Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects. Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets. Creates and validates tables...SAS
- ...Job Title Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for publication efforts and regulatory submissions. Manage the timely creation, review, completion, and delivery of statistical programming...SAS
- ...for CDISC conformance. Review Case Report Forms and eCRFs with CDISC CDASH and SDTM conformant elements. Write and manage SAS code for mapping clinical data to SDTM data structures in conformance with Emmes' SDTM Implementation Guide, project standards, and the study...SAS
- ...Minimum of 5 years of experience in using SAS to process and analyze large datasets.... ...conducting data quality reviews including clinical data, tables, graphs, and reports. # Experience... ...documentation. # SAS Certified Base Programmer certification required. # Experience...SAS
- ...Minimum of 5 years of experience in using SAS to process and analyze large datasets.... ...conducting data quality reviews including clinical data, tables, graphs, and reports. # Experience... ...documentation. # SAS Certified Base Programmer certification required. # Experience...SAS
- ...Responsibilities: Conduct statistical programming and analysis of clinical research studies. Provide programming support for... ..., biomedical, or medical device industries. Proficiency in SAS Programming, SAS Macros, R/R Studio, Clinical Trial Design, and...SASInternship
- ...Overview Clinical SAS Programmer job at cGxPServe. Princeton, NJ. Responsibilities Effectively designs and codes SAS programs using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Produces and delivers CDISC and regulatory...SAS
- ...deliverables are completed on time and of high quality. Represent the Clinical Programming function at cross-functional meetings. May... ..., or related discipline). Independently develop SAS/R programs to generate and validate datasets according to the Statistical...SASWork experience placement
- Job Title Responsibilities: Providing statistical programming support to generate tables, listings, and figures for assigned projects. Demonstrating proficiency in CDISC, SDTM, and ADaM to support various submission activities, including IA, CSR, DSUR, and publications...SAS
- Job Title Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by other functions (e.g. CRFs...SAS
- ...Major Tasks of Position: Understanding of clinical trial objectives, design, endpoints and... .... Develop programs that convert raw SAS datasets into standard format and improve... ...macros. Collaborate with manager and other programmers through participation in formal and ad-...SAS
- ...Job Title Mandatory: SDTM, SAS Looking for 5+ years of clinical SAS programmers having in depth knowledge of CDISC SDTM. Gathering data from all available source and using SAS to process it. Creating and writing programs. Preparing and presenting operations reports...SAS
- ...Job Title Responsibilities: Provides SAS programming support to all clinical studies. Manages assigned programming CROs providing oversight and appropriate QC for programming deliverables. Provides statistical programming support for regulatory submissions (e.g., FDA...SAS
- ...specifications as per SDTM/ADaM standard and study SAP. Define and create ad-hoc reports and listings for clinical teams. Develop, implement and maintain SAS programming standards. Builds/tests programs for Data Validation, Derivation, and Data Reports to...SAS
- ...Job Title Responsibilities: Develop SAS programs and statistical output for the management and reporting of clinical trial data managed by GCD. Guarantee quality of statistical output produced by external provider, to program tools to support data review activities...SAS
- ...and analysis, and reporting the results of clinical trials, including programming rules and... ...submission. Develop, debug, and enhance SAS programs to support quality control of... ...or clinical research setting as a programmer. Proficient knowledge of clinical trials...SASFor contractorsWork experience placement
- ...Sr. Statistical Programmer Responsibilities: The Sr. Statistical Programmer supports the... ...analysis datasets and statistical outputs for clinical trials. This role is key to implementing... ..., ADaM) across clinical programs. Develop and validate SAS programs to generate......SAS
- ...rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a... ...Overview Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV...SASFull timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...maintain supporting documentation. Demonstrable expertise in SAS analysis and reporting programming. Demonstrable expertise with... ..., or life science. A minimum of 5 years of relevant clinical research programming experience, 3 years specifically in the pharmaceutical...SASContract work
- ...Responsibilities: Design, code, and test SAS programs used to generate CDISC SDTM & ADaM domains and tables, listings & figures... ...equivalent related experience preferably in a pharmaceutical or clinical environment. 5+ years' experience in statistical...SAS
- ...Sciences Company, needs to hire a Statistical Programmer to provide programming support for Phase... .... Works collaboratively with Clinical Operations, Clinical Data Management, Global... ...or health related industry. dvanced SAS programming skill s and experience in other...SAS
- ...rapidly, and we are currently seeking a full-time, office-based SAS Programmer to join our Biostatistics team. This position will work on a... ...Overview Medpace Overview Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV...SASFull timeContract workWork at officeLocal areaImmediate startFlexible hours
- ...out programming activities of statistical programmers and overseeing external vendors (as... ...programming and validation activities for clinical studies and publications. Contributes... ...). ccessing and converting data to SAS from Database management system and PC...SAS
- ...most important research questions across clinical development, market access, and commercial... ...health records) Excellent programmer in R (including tidyverse) and are proficient... ...conventions, i.e. SDTM and ADaM models (using SAS) and related controlled terminologies, and...SAS
$60 - $80 per hour
...closely with Data Management and cross-functional teams to generate clinical trial metrics, support data cleaning and reconciliation... ...team PREFERRED Qualifications: Experience with Python and/or SAS in a clinical programming context Experience generating CDISC...SASContract workRemote work- ...looking for an experienced Senior Statistical Programmer to support their team. This is an... ...manipulation, analysis and reporting of primarily clinical trial data Create analysis data sets (... ...graphs (TLGs) Validate and document SAS programs and output Fulfill ad-hoc...SASRemote work
- Join to apply for the Clinical Statistical Programmer - III role at Katalyst CRO . This job was posted 8 months ago. Get AI-powered advice on this job... ...of phase I-IV clinical trial data. Proficiency in SAS/Base and SAS/Stat. Knowledge of CDISC standards: CDASH, SDTM...SASContract work
- ...programming in support of ongoing projects. Develops and/or validates SAS programs to generate SDTM/ADaM datasets following industry... ...statistical instructions. Develops and/or validates SAS programs to generate statistical output (e.g. TLFs) of clinical trial data as specified....SAS
- ...TFLs), including associated documentation like define.xml using SAS. Ensure that all programming and data are conducted in compliance... ...on a regular basis. Collaborates with Biostatisticians, Clinical Data Management, and Clinical Research Scientists on studies...SAS
$106.3k - $175k
...The Position ADS Programmer Department Summary This role is in Analytical Data Science... ...across both early- and late-stage clinical development. The Opportunity The Analytical... ...language (such as, but not limited to, SAS or R programming) and visualization/...SASWork experience placementLocal areaRelocation package